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The anomalous enrichment of the rare earth elements and yttrium (REY), U, Mo, As, Se, and V in the coal-bearing intervals intercalated within the carbonate successions in South China has attracted much attention due to the highly promising recovery potential for these elements. This study investigates the mineralogical and geochemical characteristics of the late Permian coal-bearing intervals (layers A–F) intercalated in marine carbonate strata in the Xian’an Coalfield in Guangxi Province to elucidate the mode of occurrence and enrichment process of highly elevated elements. There are two mineralogical assemblages, including quartz-albite-kaolinite-carbonates assemblage in layers D–F and quartz-illite-kaolinite-carbonates assemblage in layers A–C. Compared to the upper continental crust composition (UCC), the REY, U, Mo, As, Se, and V are predominantly enriched in layers A and B, of which layer A displays the REY–V–Se–As assemblage while layer B shows the Mo–U–V assemblage. The elevated REY contents in layer B are primarily hosted by clay minerals, zircon, and monazite; Mo, U, and V show organic association; and As and Se primarily display Fe-sulfide association. Three geological factors are most likely responsible for geochemical anomaly: (1) the more intensive seawater invasion gives rise to higher sulfur, Co, Ni, As, and Se contents, as well as higher Sr/Ba ratio in layers A–C than in layers D–F; (2) both the input of alkaline pyroclastic materials and the solution/rock interaction jointly govern the anomalous enrichment of REY; and (3) the influx of syngenetic or early diagenetic hydrothermal fluids is the predominant source of U, Mo, V, Se, and As.

The highly elevated concentrations of the rare earth elements and yttrium (REY), U, Mo, Se, and Pb in late Permian coals in some coalfields in Guangxi Province, South China, have been widely investigated; however, the mode of occurrence and enrichment mechanism of these critical elements are still under debate. This study investigates the mineralogical and geochemical compositions of coals and non-coal rocks from the Xian’an Coalfield in Guangxi Province to discuss the geological factors influencing the distribution of critical elements. The mineral in the studied coals consists mainly of quartz, and to a lesser extent, muscovite and kaolinite, with a trace amount of anatase. The coals are significantly enriched in REY, Pb, Se, Mo, and U and display the REY–U–Se–Mo–Pb-enrichment horizon (Horizon I) and U–Mo-enrichment horizon (Horizon II) adjacent to the host rocks or partings. The REY, U, Se, and Pb show organic association while Mo is primarily hosted by Fe-sulfides within Horizon I. The U and Mo have a phosphate affinity within Horizon II. Both the input of pyroclastic and epiclastic materials and the leaching of acidic solutions jointly govern the distribution of the REY–U–Se–Mo–Pb-enrichment horizon (Horizon I) and the U–Mo-enrichment horizon (Horizon II). The concentrations of REY in Horizon I exceed the cutoff grade of REY, and, therefore, the coals in the Horizon I can be regarded as promising raw materials of REY.

The behaviour and speciation of inorganic trace pollutants were studied in a 270 MWh coal-fired power station equipped with denitrification (DeNOx)-based selective catalytic reduction (SCR), electrostatic precipitators (ESP) and ammonia flue gas desulphurisation (NH3-FGD) controls. The aqueous (NH4)2SO4 slurry (pH 3.2) showed remarkably high concentrations of SO42−, Cl−, Fe, NH4+, PO43−, and F− and was substantially enriched in multiple trace pollutants, e.g. Mn, Ni, Zn, and As, which can be ascribed to the diffusion of gaseous pollutants released during combustion and to the partial dissolution of fly ash (FA) particles entrained in the flue gas FGD. These processes were favoured by the iteration of the FGD water re-circulation cycles within the scrubber. Three major unresolved performance issues remain for the NH3-FGD with respect to the retention efficiency of major and trace pollutants: (i) the high concentration of soluble salts and major and minor trace elements in the aqueous (NH4)2SO4 slurry could lead to entrainment of droplets and particles with the outgoing (OUT)-FGD gas; (ii) the ionic strength, as a result of the high concentration of the elements associated with soluble salts and major and minor elements, could lead to diminishing diffusivity of gaseous pollutants into the aqueous phase, where these are supposed to dissolve; and (iii) the acidic conditions of the aqueous (NH4)2SO4 slurry, caused by Fe-hydrolysis, could lead to low FGD efficiencies. Operating conditions at this power station affect Hg partitioning and fate across the PCC-SCR-ESP-NH3-FGD.

Superhigh organic sulfur(SHOS) coals have currently attracted great attention due to their typical depositional environments and formation history as well as their great negative impact on the ecosystem. This study investigated the geochemistry of the No. 11coalof the Late Carboniferous Taiyuan Formation from the Sangshuping coalmine, Hancheng miningarea, Weibei coalfield, Shaanxi, North China. The No. 11 coal is a high-sulfur coal with a large proportion of organic sulfur content (3.7 to 5.5%, avg. 4.4%) and belongs to typical SHOS coal. The high sulfur content in the Sangshuping coal mine has been mainly caused by the combined influences of seawater and hydrothermal fluids. The SHOS in No. 11 coal was formed in the Fe-poor and S-rich high-marine influenced occlusive environment. During the late coalification stage, a high proportion of pyritic sulfur was formed due to sufficient Fe supply from the Fe–S-rich epigenetic hydrothermal fluids. The No. 11 SHOS coal is enriched in Li–Ga–Zr–Hf and Se–Mo–Cr–V–As–Pb element assemblages. The sediment provenance of the Sangshuping coal mine is predominantly felsic–intermediate rocks from both the Yinshan and Qinling Oldland. However, the elevated concentrations of critical elements (Li, Ga, Zr, and Hf) in the No. 11 coal are primarily inherited from the Yinshan Oldland. The enrichment of the Se–Mo–Cr–V–As–Pb assemblage in No. 11 coal can be ascribed to the influence of both seawater and epigenetic hydrothermal activity.

Mineralogical and geochemical characteristics of coals provide crucial information on their potential clean, efficient, and integrated utilization. In this paper, the mineralogical and geochemical behaviors of the No. 5 coals of the Taiyuan Formation in the Weibei Coalfield, North China, were investigated, and their geological controlling factors were subsequently discussed. The minerals in the Weibei coals mainly consist of kaolinite (8.3%), calcite (5.0%), and pyrite (3.1%), with minor proportions of tobelite (2.9%), dolomite (1.7%), quartz (1.8%), and traces of siderite (0.4%) and gypsum (0.6%). Several critical elements, including Nb (19.8 mg/kg), Ta (3.6 mg/kg), Zr (71.0 mg/kg) and Li (32.3 mg/kg), occur at concentrations higher than those averages for world hard coals, making the Weibei coals potential sources of these critical elements. Several factors, terrigenous material, seawater invasion, and hydrothermal fluids are responsible for these mineralogical and geochemical characteristics. The L-type rare earth elements and yttrium (REE-Y) enrichment in the roofs and partings, Al2O3-TiO2 and Zr/TiO2-Nb/Y plots, and negative Eu and weak negative Ce anomalies in the Weibei coals indicate a felsic-intermediate dominated sediment provenance primarily derived from the Qilian-Qinling Oldland on the South. Marine bioclastic limestone, negative Ce and positive Y anomalies in coals imply the influence of seawater on the Weibei coals. Last but not least, the cleat-infilling and/or fracture-infilling calcite, pyrite, barite, and tobelite as well as the positive Eu and Gd anomalies, H-type, and M-type REE-Y enrichment patterns suggest the influence of hydrothermal fluids, which lead to re-distribution of some critical elements from roof and parting to the underlying coal seam.

We focus on a comparison of the geochemistry and mineralogy patterns found in coal, deposited dust (DD), respirable deposited dust (RDD) and inhalable suspended dust (PM10) from a number of underground mines located in China, with an emphasis on potential occupational health relevance. After obtaining the RDD from DD, a toxicological analysis (oxidative potential, OP) was carried out and compared with their geochemical patterns. The results demonstrate: i) a dependence of RDD/DD on the moisture content for high rank coals that does not exist for low rank coals; ii) RDD enrichment in a number of minerals and/or elements related to the parent coal, the wear on mining machinery, lime gunited walls and acid mine drainage; and iii) the geochemical patterns of RDD obtained from DD can be compared with PM10 with relatively good agreement, demonstrating that the characterization of DD and RDD can be used as a proxy to help evaluate the geochemical patterns of suspended PM10. With regards to the toxicological properties of RDD, the Fe content and other by-products of pyrite oxidation, as well as that of anatase, along with Si, Mn and Ba, and particle size (among others), were highly correlated with Ascorbic Acid and/or Glutathione OP.

Coal as the source of critical elements has attracted much attention and the enrichment mechanisms are of significant importance. This paper has an opportunity to investigate the mineralogical and geochemical characteristics of the Permian and Jurassic bituminous coals and associated non-coals from two underground coal mines in the Shanbei Coalfield (Northeast Ordos basin), Shaanxi Province, North China, based on the analysis of X-ray diffraction (XRD), inductively coupled plasma atomic-emission spectrometry (ICP-AES/MS), and scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS). The Jurassic and Permian coals have similar chemical features excluding ash yield, which is significantly higher in the Permian coals. Major mineral matters in the Jurassic coals are quartz, kaolinite, and calcite. By contrast, mineral assemblages of the Permian coals are dominated by kaolinite; and apatite occurring in the middle section’s partings. The Jurassic coals are only enriched in B, whereas the Permian coals are enriched in some trace elements (e.g., Nb, Ta, Th, and REY). Boron has a mixed inorganic and organic association which may be absorbed by organic matter from fluid (or groundwater) or inherited from coal-forming plants. Additionally, climatic variation also plays an important role. As for the Permian coals, kaolinite and apatite as the major carriers of elevated elements; the former were derived from the sedimentary source region (the Yinshan Oldland and the Benxi formation) and later precipitated from Ca-, and P-rich solutions. We deduced that those elevated elements may be controlled by the source rock and diagenetic fluid input. The findings of this work offered new data to figure out the mechanism of trace element enrichment of coal in the Ordos basin.

first_pagesettings Open AccessArticle Mineralogy and Geochemistry of Late Permian Coals within the Tongzi Coalfield in Guizhou Province, Southwest China by Baoqing Li 1,*,Xinguo Zhuang 1,Xavier Querol 1,2,Natalia Moreno 2OrcID,Linjian Yang 3,Yunfei Shangguan 1 andJing Li 1 1 Key Laboratory of Tectonics and Petroleum Resources (China University of Geosciences), Ministry of Education, Wuhan 430074, China 2 Institute of Environmental Assessment and Water Research, CSIC, C/Jordi Girona 18–26, 08034 Barcelona, Spain 3 No. 106 Geological Team of Guizhou Province Geology and Mineral Bureau, Zunyi 563000, China * Author to whom correspondence should be addressed. Minerals 2020, 10(1), 44; https://doi.org/10.3390/min10010044 Received: 18 December 2019 / Revised: 29 December 2019 / Accepted: 30 December 2019 / Published: 31 December 2019 (This article belongs to the Collection Minerals in Coal and Coal Combustion Products) Download PDF Browse Figures Abstract The lowermost Late Permian coal seam (C4 Coal) in the Tongzi Coalfield offers an opportunity to investigate the influence of terrigenous detrital materials from the Qianbei Upland on the mineralogical and geochemical patterns of the C4 Coal. The minerals are mainly dominated by pyrite and, to a lesser extent, tobelite, kaolinite, and calcite, along with traces of Al-oxyhydroxide minerals. The various degrees of marine influence may have resulted in the variation in the amount of Fe-sulfides (e.g., pyrite) and elements having Fe-sulfides affinity. Furthermore, the abundant Fe ions involved in the formation of Fe-sulfides were most likely derived from the claystone on the Qianbei Upland. The tobelite identified in the C4 Coal probably originated from the interaction between pre-existing kaolinite and NH4+ from NH3 released from the thermally affected organic matter at least shortly after the highly volatile bituminous stage under NH4+-rich and K+-poor conditions. The terrigenous detrital materials were derived from two pos

Previous investigations on major and trace elements within the Early Permian coals from Xinjiang Province are very scarce. This paper reports on the geochemistry of the Early Permian coals and associated non-coal rocks in the Jimunai depression, Xinjiang Province, northwestern China. Samples collected from coal exploration boreholes ZK2603, ZK3003, and ZKH1102 as well as the Haerjiao underground coal mine (Nos. HRJ-7 and HRJ-9 Coals) in the Jimunai Depression were analyzed using SEM-EDS, ICP-AES, and ICP-MS. These Early Permian coals reach the rank of semi-anthracite to anthracite and have low-sulfur contents (0.30% on average). In comparison with the average element concentrations of world coals, Zr, Hf, and rare earth elements and Y (REY) are slightly enriched (concentration coefficient (CC) = 2–5, as the ratio of element content in sample vs. that in world coals) and Mn is enriched (CC = 5–10) in the ZK2603, ZK3003, and ZKH1102 coals. Niobium and Ta are highly enriched in the ZK2603 and ZK3003 coals (CC = 10–100). The HRJ-7 and HRJ-9 coals are slightly enriched in Mn (CC = 2–5). The coals have a sediment source region mainly composed of intermediate-felsic compositions from the Saur Volcanic Arc to the south of the Jimunai Depression, which may have provided relatively high geochemical background concentrations of Zr, Hf, Nb, and Ta. Manganese is hosted mainly in ankerite that was derived from epigenetic precipitation from Mn-bearing hydrothermal fluids. Zirconium and Hf in the ZK2603, ZK3003, and ZKH1102 coals are controlled primarily by detrital matter or hydrothermal fluids, the latter of which results in the higher Zr/Hf ratio in the ZK2603 and ZK3003 coals due to the re-distribution of Zr and Hf. Niobium and Ta in the ZK2603 and ZK3003 coals are concentrated chiefly in zircon, and hydrothermal fluid activity caused the release of Nb and Ta from previously-existing inorganic constituents and subsequent incorporation into zircon, resulting in the lower Nb/Ta r

This paper investigates the mineralogy of coal and non-coal samples from the Haerjiao exploration area in the Jimunai depression, Xinjiang Uygur Autonomous Region, northwestern China, using X-ray diffraction (XRD), optical microscopy and scanning electron microscopy with an energy dispersive X-ray spectrometer (SEM-EDX). The minerals in the anthracite proximal to the igneous intrusions are represented by the occurrence of chlorite, muscovite, and illite, which are absent in the semianthracite distal to the igneous intrusions. Kaolinite, the dominant mineral in the semianthracite, decreases in abundance or even disappears in the anthracite. Muscovite and illite in the anthracite are interpreted to result from the alteration of the kaolinite precursor and possibly formed by the interaction of kaolinite and elements (e.g., K, Fe, and Mg) from igneous hydrothermal solutions. The formation of chlorite is the result of the transformation of kaolinite due to the interaction of kaolinite with Fe-Mg-rich solutions during the diagenetic stage and the direct epigenetic precipitation from Fe-Mg-rich igneous siliceous hydrothermal fluids. Calcite, ankerite, and sulfide minerals resulted from epigenetic precipitation from hydrothermal fluids. Cleat/fracture mineralization indicates that the Fe-Mg-rich hydrothermal fluid from which chlorite precipitated was introduced earlier than the Ca-rich fluid from which calcite precipitated. The injection of hydrothermal solutions that formed sulfide minerals occurred at the latest stage. © 2019

The mineralogical and geochemical characteristics of feed coals and coal combustion products (CCPs) from the Shenhuo and Yihua Power Plants in Xinjiang Autonomous Region, were studied by means of proximate analysis, Power X-ray diffraction (XRD), scanning electron microscopy with Energy Dispersive X-ray analyzer (SEM-EDX), inductively coupled plasma atomic emission spectrometry (ICP-MS) and inductively coupled plasma mass spectrometry (ICP-AES). The environmental geochemistry of CCPs was evaluated by Al-normalized enrichment factor as well as European Standard EN-12457 leaching test. Two feed coals have the characteristics of low sulfur content, medium to high volatiles matter yields, medium moisture content, super low to medium ash yield, medium to high calorific value and low mineral content. The main crystalline facies in fly ash and slag are quartz and mullite, with a small amount of calcite, and some unburned carbon. Hematite, SrSO4 and barite also can be observed in fly ashes by SEM. Typical plerophere occurs in fine fly ash rather than the coarse fly ash. The concentration of most trace elements in CCPs falls within the lower concentration range of European fly ashes. With respect to the partitioning behavior of trace elements during coal combustion, S is highly volatile, and Mg, Na, Zn, B, Co, As, Nb, Zr, Cu and K also show certain volatility, which may to some extent emit to the atmosphere. Furthermore, leaching experiments show that leachable concentrations of most of the potentially toxic elements in CCPs are low, and the CCPs fall in the range between inert and nonhazardous landfill material regulated by the 2003/33/EC Decision.